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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172285Generated: October 31, 2026

Dichloromethane → tert-Butyl 4-(2-oxo-1,4-dihydroquinazolin-3(2H)-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1172285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantEthyl AcetateHCID 8857—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactanttert-Butyl 4-{[(2-nitrophenyl)methyl]amino}piperidine-1-carboxylateHCID 13046886—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 4-(2-oxo-1,4-dihydroquinazolin-3(2H)-yl)piperidine-1-carboxylateHCID 5341530324.4%

Reaction Steps

To a solution of tert-butyl 4-(2-nitrobenzylamino)piperidine-1-carboxylate (13.2 g, 43.2 mmol) in THF (400 ml) was added a solution of CDI (7.7 g, 47.5 mmol) in 1:1 DCM: THF (100 ml) dropwise over 1 hour followed by stirring the reaction mixture for a further 16 hours. The reaction mixture was evaporated to give an oil that, when treated with EtOAc, precipitated the desired product. The precipitate was washed with cold EtOAc and dried to give a yellow solid (3.5 g). LC/MS (10% to 99%): M/Z (M+H)+ (obs)=332; tR=3.01.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834000B2
Source datasetuspto-grants-2010_11
ORD IDord-09d3c9277dbd4306b846f92f6906310a
Source noteuspto-grants-2010_11